Cross-talk between non-coding RNAs and PI3K/AKT/mTOR pathway in colorectal cancer

Zeinab Moafian1, Abolfazl Maghrouni2, Arash Soltani3

  • 1Protein Chemistry Laboratory (PCL), Department of Biology, College of Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.

Insights

This review explores how non-coding RNAs regulate the PI3K/AKT/mTOR pathway in colorectal cancer (CRC). Understanding these interactions may reveal new diagnostic and therapeutic targets for CRC treatment.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Colorectal cancer (CRC) is a leading cause of cancer mortality worldwide, with metastasis being a primary driver.
  • Current CRC treatments face limitations, necessitating the development of novel therapeutic strategies.
  • The biochemical mechanisms underlying CRC progression remain incompletely understood.

Purpose of the Study:

  • To review the role of non-coding RNAs (ncRNAs) in the development and progression of colorectal cancer.
  • To elucidate the regulatory functions of ncRNAs on the PI3K/AKT/mTOR pathway in CRC.
  • To explore the potential of ncRNAs as diagnostic biomarkers and therapeutic targets for CRC.

Main Methods:

  • Literature review focusing on non-coding RNAs (lncRNAs, miRNAs) and their involvement in CRC.
  • Analysis of the PI3K/AKT/mTOR signaling pathway in the context of CRC.
  • Synthesis of current research on ncRNA-mediated regulation of cancer-related pathways.

Main Results:

  • Non-coding RNAs, including long non-coding RNAs (lncRNAs) and microRNAs (miRNAs), play significant roles in CRC development and progression.
  • Dysregulation of the PI3K/AKT/mTOR pathway is common in cancers, including CRC.
  • Specific ncRNAs have been identified as key regulators of the PI3K/AKT/mTOR pathway in CRC, influencing tumor growth and metastasis.

Conclusions:

  • Non-coding RNAs are critical regulators of the PI3K/AKT/mTOR pathway in colorectal cancer.
  • Targeting ncRNAs involved in this pathway presents a promising avenue for novel CRC diagnostics and therapeutics.
  • Further research into the precise mechanisms of ncRNAs in CRC is warranted to optimize clinical applications.

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